Functional organic material decomposing agent and preparation method thereof
A decomposing agent and bacterial agent technology, which is applied in the field of agricultural microbial preparations, can solve problems such as undiscovered, and achieve the effects of long storage period, suppression of soil-borne diseases, and good soil
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] The preparation of embodiment 1 Streptomyces flexneri CGMCC No.5133 original bacterial agent
[0032] The present invention adopts the liquid-solid combined fermentation culture process to carry out the culture of Streptomyces freundii CLIMAX-VSF, through the first liquid multiplication culture and then inserting into the solid culture multiplication culture, the specific steps include:
[0033] 1) Seed preparation and liquid multiplication culture: first activate the freeze-dried tube containing Streptomyces flexneri CLIMAX-VSF. The specific method is to first insert it into the slant of Gao’s No. 1 medium and cultivate it at 30±2°C for 15 days; after obtaining healthy colonies, insert it into PDA medium and cultivate it at 30°C for 5 days, and then select healthy colonies. The strains were inserted into a sterilized liquid medium consisting of 20 parts of sucrose, 5 parts of sodium chloride, 20 parts of peptone, 5 parts of magnesium sulfate, 3 parts of potassium dihyd...
Embodiment 2
[0036] The preparation of embodiment 2 Myceliophthora thermophila CGMCC No.5134 original bacterial agent
[0037] 1) Seed preparation and liquid proliferation culture: first activate the freeze-dried tube containing Myceliophthora thermophila CGMCC No.5134, the specific method is to first connect the bacteria in the freeze-dried tube to the PDA on the aseptic operating table Cultivate at 42°C for 5 days on the slant of the medium; after obtaining healthy colonies, insert them into nutrient agar medium and culture at 42°C for 5 days, then select healthy strains for development and insert them into sterilized sucrose 10 1 part, 5 parts of sodium chloride, 10 parts of beef extract, 5 parts of calcium chloride, 0.5 part of potassium dihydrogen phosphate, 0.01 part of ferric chloride, 2 parts of yeast extract, and 1000 parts of water. 150r / min, cultured at 42°C for 3 days to obtain Myceliophthora thermophila seed liquid.
[0038] 2) Solid proliferation culture: insert the Myceliop...
Embodiment 3
[0040] The preparation of embodiment 3 Trichoderma viridans ACCC 30169 original bacterial agent
[0041]1) Seed preparation and liquid proliferation culture: first activate the freeze-dried tube containing Trichoderma viride ACCC30169 (purchased from the China Agricultural Microorganism Culture Collection Management Center), the specific method is to first put the freeze-dried tube in the aseptic operation table The strains were inserted into the slant of PDA medium and cultured at 30±2°C for 5 days; after obtaining healthy colonies, they were inserted into nutrient agar medium, cultured at 30±2°C for 5 days, and then selected The healthy strains were inserted into the sterilized 10 parts of sucrose, 10 parts of sweet potato juice, 5 parts of sodium chloride, 10 parts of peptone, 5 parts of magnesium sulfate, 0.5 parts of potassium dihydrogen phosphate, 3 parts of ammonium sulfate, and 1000 parts of water. In a liquid medium composed of parts, and cultivated at 150r / min, 30±2°...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com